Reaction of monoterpene hydroxy thiols with chlorine dioxide
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| 024 | 7 | 0 | |a 10.1134/S1070428015100012 |2 doi |
| 035 | |a (NATIONALLICENCE)springer-10.1134/S1070428015100012 | ||
| 245 | 0 | 0 | |a Reaction of monoterpene hydroxy thiols with chlorine dioxide |h [Elektronische Daten] |c [O. Lezina, O. Grebenkina, D. Sudarikov, Yu. Krymskaya, S. Rubtsova, A. Kutchin] |
| 520 | 3 | |a Reactions of isobornane and pinane hydroxy thiols with chlorine dioxide have been studied. Unlike pinane derivatives, hydroxy thiols of the isobornane series reacted with chlorine dioxide to give the corresponding sulfinyl derivatives with high stereoselectivity. New terpenoids containing sulfur, oxygen, and chlorine atoms have been synthesized by oxidation of hydroxy thiols with chlorine dioxide. | |
| 540 | |a Pleiades Publishing, Ltd., 2015 | ||
| 700 | 1 | |a Lezina |D O. |u Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia |4 aut | |
| 700 | 1 | |a Grebenkina |D O. |u Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia |4 aut | |
| 700 | 1 | |a Sudarikov |D D. |u Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia |4 aut | |
| 700 | 1 | |a Krymskaya |D Yu |u Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia |4 aut | |
| 700 | 1 | |a Rubtsova |D S. |u Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia |4 aut | |
| 700 | 1 | |a Kutchin |D A. |u Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia |4 aut | |
| 773 | 0 | |t Russian Journal of Organic Chemistry |d Pleiades Publishing |g 51/10(2015-10-01), 1359-1367 |x 1070-4280 |q 51:10<1359 |1 2015 |2 51 |o 11178 | |
| 856 | 4 | 0 | |u https://doi.org/10.1134/S1070428015100012 |q text/html |z Onlinezugriff via DOI |
| 898 | |a BK010053 |b XK010053 |c XK010000 | ||
| 900 | 7 | |a Metadata rights reserved |b Springer special CC-BY-NC licence |2 nationallicence | |
| 908 | |D 1 |a research-article |2 jats | ||
| 949 | |B NATIONALLICENCE |F NATIONALLICENCE |b NL-springer | ||
| 950 | |B NATIONALLICENCE |P 856 |E 40 |u https://doi.org/10.1134/S1070428015100012 |q text/html |z Onlinezugriff via DOI | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Lezina |D O. |u Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Grebenkina |D O. |u Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Sudarikov |D D. |u Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Krymskaya |D Yu |u Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Rubtsova |D S. |u Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Kutchin |D A. |u Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia |4 aut | ||
| 950 | |B NATIONALLICENCE |P 773 |E 0- |t Russian Journal of Organic Chemistry |d Pleiades Publishing |g 51/10(2015-10-01), 1359-1367 |x 1070-4280 |q 51:10<1359 |1 2015 |2 51 |o 11178 | ||